Carisoprodol

Product NDC

50090-2530

11-digit product format

500902530

Labeler code

50090

Product ID

50090-2530_6b94043a-ebe0-457b-99a2-c0ea44974a0d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carisoprodol

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040245

Marketing category

ANDA

Marketing start

1997-09-08

Marketing end

0000-00-00

Substance

CARISOPRODOL

Active strength

350 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record